Comment to: Hepcidin: From discovery to differential diagnosis. Haematologica 2008; 93:90-7

Haematologica

Volumn 93, Issue 6, 2008, Pages

  Olsson, K Sigvard ^a   Norrby, Anders ^a  

^a SAHLGRENSKA UNIVERSITY HOSPITAL   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

HEMOGLOBIN; HEPCIDIN;

ANEMIA; BLOOD VOLUME; BONE MARROW; DIFFERENTIAL DIAGNOSIS; ERYTHROCYTE; HEMATOCRIT; IRON METABOLISM; IRON STORAGE; MACROPHAGE; NOTE; PHLEBOTOMY;

ANEMIA; BLOOD CHEMICAL ANALYSIS; CHEMISTRY, CLINICAL; GENE EXPRESSION REGULATION; HUMANS; IRON; IRON METABOLISM DISORDERS; MALE; MODELS, BIOLOGICAL; PHLEBOTOMY;

EID: 44949185314     PISSN: 03906078     EISSN: None     Source Type: Journal    
DOI: 10.3324/haematol.12814     Document Type: Note

References (5)

1. Kemna EH, Tjalsma H, Willems HL, Swinkels DW. Hepcidin: from discovery to differential diagnosis. Haematologica 2008;93:90-7.
2. Swinkels DW, Janssen MC, Bergmans J, Marx JJ. Hereditary hemochromatosis: genetic complexity and new diagnostic approaches. Clin Chem 2006;52:950-68.
3. Andrews NC. Disorders of iron metabolism. N Engl J Med 1999;341:1986-95.
4. Olsson KS. Iron stores in normal men and male blood donors. As measured by desferrioxamine and quantitative phlebotomy. Acta Med Scand 1972;192:401-7.
5. Norrby A. Iron absorption studies in iron deficiency. Scand J Haematol Suppl 1974;20:1-125.